A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052675



Internal ID19141894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102105789..102280443hg38UCSC Ensembl
Innerchr9:104868071..105042725hg19UCSC Ensembl
Innerchr9:103907892..104082546hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38174655
hg19174655
hg18174655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697579
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052675
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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